GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SMc04256 in Dinoroseobacter shibae DFL-12

Align ABC transporter for D-Cellobiose and D-Salicin, ATPase component (characterized)
to candidate 3607949 Dshi_1357 ABC transporter related (RefSeq)

Query= reanno::Smeli:SMc04256
         (361 letters)



>FitnessBrowser__Dino:3607949
          Length = 349

 Score =  290 bits (743), Expect = 3e-83
 Identities = 170/357 (47%), Positives = 219/357 (61%), Gaps = 14/357 (3%)

Query: 1   MTSVSVRDLSLNFGAVTVLDRLNLDIDHGEFLVLLGSSGCGKSTLLNCIAGLLDVSDGQI 60
           M ++++  +   FG V V+  ++L+I  GEF+V +G SGCGKSTLL  I GL D S G +
Sbjct: 1   MGAITLSKVEKWFGDVQVIKGVDLEIRDGEFVVFVGPSGCGKSTLLRMIGGLEDTSRGAM 60

Query: 61  FIKDRNVTWEEPKDRGIGMVFQSYALYPQMTVEKNLSFGLKVAKIPPAEIEKRVKRASEI 120
            I   +VT   P  RG+ MVFQSYALYP M+V +N+ F LK A  P AEI ++V+ A+ +
Sbjct: 61  LIDGVDVTDHPPAKRGLTMVFQSYALYPHMSVRENMGFSLKTAGAPAAEIAEKVEAAAAV 120

Query: 121 LQIQPLLKRKPSELSGGQRQRVAIGRALVRDVDVFLFDEPLSNLDAKLRSELRVEIKRLH 180
           L+++P L R+P +LSGGQRQRVAIGR++VR    FLFDEPLSNLDA LR E+R EI +LH
Sbjct: 121 LKLEPYLDRRPKDLSGGQRQRVAIGRSIVRAPTAFLFDEPLSNLDAALRVEMRYEIAKLH 180

Query: 181 QSLKNTMIYVTHDQIEALTLADRIAVMKSGVIQQLADPMTIYNAPENLFVAGFIGSPSMN 240
           QSL  TMIYVTHDQ+EA+TLADRI V++ G I Q+  P  +Y  P NLFVA FIGSP MN
Sbjct: 181 QSLDTTMIYVTHDQVEAMTLADRIVVLEFGKIAQVGTPRELYETPANLFVAQFIGSPKMN 240

Query: 241 FFRGEVEPKDGRSFVRAGGIAFDVTAYPAHTRLQPGQKVVLGLRPEHVKVDEARDGEPTH 300
                 +   GR  + AG         PA         V LG+RPEH  +     G    
Sbjct: 241 VMPCTTDA--GRYRLSAGRGGVFSGDRPA---------VQLGIRPEH--ITPGAPGTGAC 287

Query: 301 QAVVDIEEPMGADNLLWLTFAGQS-MSVRIAGQRRYPPGSTVRLSFDMGVASIFDAE 356
              VD+ E +GAD LL L    +  ++VR+ G     PG  V LSF+    S FD +
Sbjct: 288 DGRVDVVEYLGADTLLVLDCGPEGRVTVRVIGDTDLTPGDAVGLSFNPDRLSFFDTD 344


Lambda     K      H
   0.320    0.137    0.392 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 383
Number of extensions: 14
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 361
Length of database: 349
Length adjustment: 29
Effective length of query: 332
Effective length of database: 320
Effective search space:   106240
Effective search space used:   106240
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory